期刊文献+

一种铁催化的四氟硼酸芳基重氮盐合成联苯类化合物方法的研究

Ferrum Catalyzed Coupling Reaction of Arenediazonium Tetrafluoroborates
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摘要 一种简单高效的在温和条件下用四氟硼酸芳基重氮盐和铁盐在四氯化碳溶剂中进行的自身偶联反应,可以以较高的产率得到各种自身偶联的联苯类化合物。 A simple and efficient protocol has been developed for the synthesis of various symmetrical biaryls in good to excellent yields from the homocoupling reactions of arenediazonium salts with ferrous salt in carbon tetrachloride solution under mild reaction conditions.
出处 《浙江化工》 CAS 2012年第11期4-6,共3页 Zhejiang Chemical Industry
关键词 偶联反应 铁盐 四氟硼酸芳基重氮盐 coupling reaction ferrous salt arenediazonium tetrafluoroborates
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参考文献3

  • 1Bfingmann G, Breuning M, Tasler S. The Lactone Concept: An Efficient Pathway to Axially Chiral Natural Products and Useful Reagents [J]. Synthesis, 1999, 525-558.
  • 2Nelson T D, Crouch R D. Cu, Ni, and Pd Mediated Homocoupling Reactions in Biaryl Syntheses: The Ullmann Reaction [J]. Org. React. 2004, 63: 265-556.
  • 3Robinson M K, Kochurina V S, Hanna J J M. Palladium-catalyzed homocoupling of arenediazonium salts: an operationally simple synthesis of symmetrical biaryls []]. Tetrahedron Lett; 2007, 48: 7687-7690.

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